What is the 2,7-Pyrenedicarboxylic acid?

2,7-Pyrenedicarboxylic acid is , while it's Molecular Formula is C18H10O4. Used in Organic Synthesis: 2,7-Pyrenedicarboxylic acid is used as a precursor in the synthesis of various organic compounds, leveraging its reactive carboxylic acid groups for the formation of esters, amides, and other functional groups. Used in Bioimaging Studies: As a fluorescent probe, 2,7-PDA is utilized in bioimaging studies to visualize and track specific biological processes or molecules within living organisms, taking advantage of its strong fluorescence under UV light. Used in Material Science: 2,7-Pyrenedicarboxylic acid is employed in the development of functional organic materials and electronic devices, such as organic light-emitting diodes (OLEDs) and organic field-effect transistors (OFETs), due to its unique optical and electronic properties. Used in Environmental Science: 2,7-PDA is of interest to environmental scientists as a marker for identifying sources of PAH pollution, given its presence in atmospheric aerosols. This aids in understanding the environmental impact and potential health risks associated with PAH exposure.

What is the CAS number for 2,7-Pyrenedicarboxylic acid?

The CAS number of 2,7-Pyrenedicarboxylic acid is 214622-81-8.

What is 2,7-Pyrenedicarboxylic acid (214622-81-8) used for?

2,7-Pyrenedicarboxylic acid, also known as 2,7-PDA, is a polycyclic aromatic hydrocarbon (PAH) compound characterized by two carboxylic acid groups attached to a central pyrene ring. This yellow crystalline solid exhibits strong fluorescence under UV light and is insoluble in water. Its unique optical and electronic properties make it a valuable precursor in the synthesis of various organic compounds and a promising fluorescent probe in bioimaging studies.

What is the 2,7-Pyrenedicarboxylic acid?

2,7-Pyrenedicarboxylic acid is , while it's Molecular Formula is C18H10O4. Used in Organic Synthesis: 2,7-Pyrenedicarboxylic acid is used as a precursor in the synthesis of various organic compounds, leveraging its reactive carboxylic acid groups for the formation of esters, amides, and other functional groups. Used in Bioimaging Studies: As a fluorescent probe, 2,7-PDA is utilized in bioimaging studies to visualize and track specific biological processes or molecules within living organisms, taking advantage of its strong fluorescence under UV light. Used in Material Science: 2,7-Pyrenedicarboxylic acid is employed in the development of functional organic materials and electronic devices, such as organic light-emitting diodes (OLEDs) and organic field-effect transistors (OFETs), due to its unique optical and electronic properties. Used in Environmental Science: 2,7-PDA is of interest to environmental scientists as a marker for identifying sources of PAH pollution, given its presence in atmospheric aerosols. This aids in understanding the environmental impact and potential health risks associated with PAH exposure.

What is the CAS number for 2,7-Pyrenedicarboxylic acid?

The CAS number of 2,7-Pyrenedicarboxylic acid is 214622-81-8.

What is 2,7-Pyrenedicarboxylic acid (214622-81-8) used for?

2,7-Pyrenedicarboxylic acid, also known as 2,7-PDA, is a polycyclic aromatic hydrocarbon (PAH) compound characterized by two carboxylic acid groups attached to a central pyrene ring. This yellow crystalline solid exhibits strong fluorescence under UV light and is insoluble in water. Its unique optical and electronic properties make it a valuable precursor in the synthesis of various organic compounds and a promising fluorescent probe in bioimaging studies.

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2,7-Pyrenedicarboxylic acid

Name 2,7-Pyrenedicarboxylic acid
CAS 214622-81-8
Purity 99%

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Product Details

99% Purity Commercial production 2,7-Pyrenedicarboxylic acid 214622-81-8 with Cheapest Price

Molecular Formula: C18H10O4
Molecular Weight: 290.275
PSA： 74.60000
LogP: 3.98040

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214622-81-8 Process route

: 124-38-9,18923-20-1
carbon dioxide

: 102587-98-4
2,7-dibromo-4,5,9,10-tetrahydropyrene

: 214622-81-8
pyrene-2,7-dicarboxylic acid

Conditions

Conditions	Yield
With n-butyllithium; In diethyl ether; at -78 - 20 ℃; Acidic conditions;	96%
2,7-dibromo-4,5,9,10-tetrahydropyrene; With n-butyllithium; In tetrahydrofuran; hexane; at -78 ℃; for 0.5h; Inert atmosphere; carbon dioxide; In tetrahydrofuran; hexane; at 20 ℃; Inert atmosphere;	91%
With n-butyllithium; In tetrahydrofuran; at -78 ℃;

: 129-00-0
pyrene

: 214622-81-8
pyrene-2,7-dicarboxylic acid

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: (1,5-cyclooctadiene)(methoxy)iridium(I) dimer; 4,4'-di-tert-butyl-2,2'-bipyridine / tetrahydrofuran / 16 h / 80 °C / Inert atmosphere 2: copper(ll) bromide / tetrahydrofuran; methanol; water / 16 h / 90 °C 3: n-butyllithium / diethyl ether / -78 - 20 °C / Acidic conditions With n-butyllithium; (1,5-cyclooctadiene)(methoxy)iridium(I) dimer; 4,4'-di-tert-butyl-2,2'-bipyridine; copper(ll) bromide; In tetrahydrofuran; methanol; diethyl ether; water;
Multi-step reaction with 3 steps 1.1: (1,5-cyclooctadiene)(methoxy)iridium(I) dimer; 4,4'-di-tert-butyl-2,2'-bipyridine / tetrahydrofuran / 16 h / 80 °C / Schlenk technique; Inert atmosphere; Sealed tube 2.1: copper(ll) bromide / tetrahydrofuran; methanol; water / 90 °C 3.1: n-butyllithium / tetrahydrofuran; hexane / 0.5 h / -78 °C / Inert atmosphere 3.2: 20 °C / Inert atmosphere With n-butyllithium; (1,5-cyclooctadiene)(methoxy)iridium(I) dimer; 4,4'-di-tert-butyl-2,2'-bipyridine; copper(ll) bromide; In tetrahydrofuran; methanol; hexane; water;

Yield

Multi-step reaction with 3 steps

1: (1,5-cyclooctadiene)(methoxy)iridium(I) dimer; 4,4'-di-tert-butyl-2,2'-bipyridine / tetrahydrofuran / 16 h / 80 °C / Inert atmosphere

2: copper(ll) bromide / tetrahydrofuran; methanol; water / 16 h / 90 °C

3: n-butyllithium / diethyl ether / -78 - 20 °C / Acidic conditions

With n-butyllithium; (1,5-cyclooctadiene)(methoxy)iridium(I) dimer; 4,4'-di-tert-butyl-2,2'-bipyridine; copper(ll) bromide; In tetrahydrofuran; methanol; diethyl ether; water;

Multi-step reaction with 3 steps

1.1: (1,5-cyclooctadiene)(methoxy)iridium(I) dimer; 4,4'-di-tert-butyl-2,2'-bipyridine / tetrahydrofuran / 16 h / 80 °C / Schlenk technique; Inert atmosphere; Sealed tube

2.1: copper(ll) bromide / tetrahydrofuran; methanol; water / 90 °C

3.1: n-butyllithium / tetrahydrofuran; hexane / 0.5 h / -78 °C / Inert atmosphere

3.2: 20 °C / Inert atmosphere

With n-butyllithium; (1,5-cyclooctadiene)(methoxy)iridium(I) dimer; 4,4'-di-tert-butyl-2,2'-bipyridine; copper(ll) bromide; In tetrahydrofuran; methanol; hexane; water;

214622-81-8 Upstream products

129-00-0
pyrene
124-38-9
carbon dioxide
102587-98-4
2,7-dibromo-4,5,9,10-tetrahydropyrene

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